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E Tournier

Showing results (91-100 of 155) with videos related to

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Medicine|June 5, 2001
Familial lupus erythematosus. Clinical and immunologic features of 125 multiplex familiesM Michel, C Johanet, O Meyer, et al.
Neuropediatrics|November 24, 1999
Recurrent episodes of coma: an unusual phenotype of familial hemiplegic migraine with linkage to chromosome 1B Echenne, A Ducros, F Rivier, et al.
Neurology|August 26, 1998
Patterns of MRI lesions in CADASILH Chabriat, C Levy, H Taillia, et al.
Annales De Dermatologie Et De Venereologie|April 22, 2018
[Dermatologic toxicities of immune checkpoint inhibitors]V Sibaud, S Boulinguez, C Pagès, et al.
Annals of Neurology|November 1, 1995
Familial hemiplegic migraine and autosomal dominant arteriopathy with leukoencephalopathy (CADASIL)M Hutchinson, J O'Riordan, M Javed, et al.
Journal of Immunology (Baltimore, Md. : 1950)|May 15, 1996
TCR alpha beta gene usage for myelin basic protein recognition in healthy monozygous twinsA Shanmugam, C Copie-Bergman, B Falissard, et al.
Neurology|November 4, 2000
CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophyK Vahedi, C Denier, A Ducros, et al.
Annals of Neurology|March 1, 1995
A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19pK Vahedi, A Joutel, P Van Bogaert, et al.
European Journal of Immunology|October 1, 1994
Healthy monozygous twins do not recognize identical T cell epitopes on the myelin basic protein autoantigenA Shanmugam, C Copie-Bergman, G Hashim, et al.
The Journal of Clinical Investigation|March 11, 2000
The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patientsA Joutel, F Andreux, S Gaulis, et al.
Pageof 16

Showing results (91-100 of 155) with videos related to

Sort By:
Pageof 16
Medicine|June 5, 2001
Familial lupus erythematosus. Clinical and immunologic features of 125 multiplex familiesM Michel, C Johanet, O Meyer, et al.
Neuropediatrics|November 24, 1999
Recurrent episodes of coma: an unusual phenotype of familial hemiplegic migraine with linkage to chromosome 1B Echenne, A Ducros, F Rivier, et al.
Neurology|August 26, 1998
Patterns of MRI lesions in CADASILH Chabriat, C Levy, H Taillia, et al.
Annales De Dermatologie Et De Venereologie|April 22, 2018
[Dermatologic toxicities of immune checkpoint inhibitors]V Sibaud, S Boulinguez, C Pagès, et al.
Annals of Neurology|November 1, 1995
Familial hemiplegic migraine and autosomal dominant arteriopathy with leukoencephalopathy (CADASIL)M Hutchinson, J O'Riordan, M Javed, et al.
Journal of Immunology (Baltimore, Md. : 1950)|May 15, 1996
TCR alpha beta gene usage for myelin basic protein recognition in healthy monozygous twinsA Shanmugam, C Copie-Bergman, B Falissard, et al.
Neurology|November 4, 2000
CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophyK Vahedi, C Denier, A Ducros, et al.
Annals of Neurology|March 1, 1995
A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19pK Vahedi, A Joutel, P Van Bogaert, et al.
European Journal of Immunology|October 1, 1994
Healthy monozygous twins do not recognize identical T cell epitopes on the myelin basic protein autoantigenA Shanmugam, C Copie-Bergman, G Hashim, et al.
The Journal of Clinical Investigation|March 11, 2000
The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patientsA Joutel, F Andreux, S Gaulis, et al.
Pageof 16